ClinVar Miner

Submissions for variant NM_020719.3(PRR12):c.695dup (p.Asp233fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics laboratory, Necker Hospital RCV003325356 SCV004031319 likely pathogenic not provided 2019-01-29 no assertion criteria provided clinical testing

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